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Get the free Automated External Defibrillator (aed) Application

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This form is used to apply for an Automated External Defibrillator (AED) donation from the Henry Angell - James Memorial Trust, specifically for organizations in the West Midlands. Applicants must provide information about their facility, reasons for requesting an AED, and the ability to maintain it.
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How to fill out automated external defibrillator aed

01
Ensure the AED is turned on.
02
Open the AED's pads case.
03
Remove clothing from the person's chest to expose skin.
04
Attach the adhesive pads to the bare chest, following the diagrams on the pads.
05
Ensure no one is touching the person and press the shock button if advised by the AED.
06
Follow additional prompts from the AED, including performing CPR if advised.

Who needs automated external defibrillator aed?

01
Individuals experiencing sudden cardiac arrest.
02
Event organizers of places with high foot traffic such as schools, malls, and sports venues.
03
Emergency response teams.
04
Healthcare providers in clinical settings.
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An Automated External Defibrillator (AED) is a portable medical device that diagnoses and treats certain life-threatening cardiac arrhythmias through defibrillation, allowing the heart to re-establish an effective rhythm.
Requirements for filing an automated external defibrillator (AED) may vary by jurisdiction, but typically, facilities that are required to have an AED include schools, gyms, and public venues. Certain healthcare professionals may also be required to file AED use reports.
To fill out an AED log, document the date and time of use, the location, any observations during the event, the outcome, and any maintenance checks performed before or after use.
The purpose of an Automated External Defibrillator (AED) is to provide rapid treatment to individuals experiencing sudden cardiac arrest, increasing the chances of survival through timely defibrillation.
Information that must be reported on an AED includes the date and time of use, the outcomes of the intervention, patient details if applicable, and any maintenance or servicing information for the device.
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